EP0070395A2 - Procédé de préparation de 3-cyanopyridine - Google Patents

Procédé de préparation de 3-cyanopyridine Download PDF

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Publication number
EP0070395A2
EP0070395A2 EP82105359A EP82105359A EP0070395A2 EP 0070395 A2 EP0070395 A2 EP 0070395A2 EP 82105359 A EP82105359 A EP 82105359A EP 82105359 A EP82105359 A EP 82105359A EP 0070395 A2 EP0070395 A2 EP 0070395A2
Authority
EP
European Patent Office
Prior art keywords
ammonia
water
gas
cyanopyridine
methylpyridine
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP82105359A
Other languages
German (de)
English (en)
Other versions
EP0070395A3 (en
EP0070395B1 (fr
Inventor
Helmut Beschke
Franz Ludwig Dipl.-Ing. Dahm
Heinz Dr. Dipl.-Chem. Friedrich
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Evonik Operations GmbH
Original Assignee
Degussa GmbH
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Degussa GmbH filed Critical Degussa GmbH
Priority to AT82105359T priority Critical patent/ATE22075T1/de
Publication of EP0070395A2 publication Critical patent/EP0070395A2/fr
Publication of EP0070395A3 publication Critical patent/EP0070395A3/de
Application granted granted Critical
Publication of EP0070395B1 publication Critical patent/EP0070395B1/fr
Expired legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/84—Nitriles

Definitions

  • the invention relates to a process for obtaining 3-cyanopyridine from the gas mixtures obtained in the catalytic reaction of 3-methylpyridine with ammonia and oxygen.
  • Catalysts which are produced by mixing mixtures containing antimony and vanadium and at least one of the elements titanium, iron, copper, cobalt, manganese and nickel and optionally a carrier substance by heating to temperatures of 600 to 11.00 ° C. are particularly suitable Pretreated in the presence of oxygen (DE-PS 2 039 497).
  • the gas mixtures formed in the catalytic reaction generally contain - regardless of which catalyst is used - 3-cyanopyridine, ammonia, possibly unreacted 3-methylpyridine and by-products such as water, carbon dioxide, Nicotinamide and hydrogen cyanide.
  • the work-up is essentially aimed at the recovery of 3-cyanopyridine and the recovery of the excess ammonia and the unreacted 3-methylpyridine. In order for the ammonia to be recycled and reused, it is necessary to separate it from carbon dioxide and the other by-products.
  • reaction mixture is washed at low temperature with methanol and in this way the 3-cyanopyridine, any 3-methylpyridine present and some ammonia are separated off (DE-OS 2 435 344).
  • the main parts of ammonia remain in the residual gas.
  • this also contains by-products, such as carbon dioxide in particular, which accumulate and interfere with the reaction if the residual gas is repeatedly circulated leads.
  • a process has now been found for obtaining 3-cyanopyridine from the gas mixtures obtained in the catalytic reaction of 3-methylpyridine with ammonia and oxygen by treating them with water, which is characterized in that the gas mixtures are initially at temperatures from 30 to 60 ° C and then at about 10 to 30 ° C lower temperatures. In this way it is possible not only to obtain pure 3-cyanopyridine, but also to separate and recover the ammonia and any 3-methylpyridine present in such a way that these substances can be recycled immediately and without loss.
  • the 3-cyanopyridine can be obtained from all gas mixtures which are obtained in the usual catalytic reactions of 3-methylpyridine with ammonia and oxygen in the gas phase, in particular from the gas mixtures which are used in the reaction using the catalysts according to DE -OS 2 039 497 or DE-OS 3 107 755 arise.
  • the warm gas mixtures are expediently raised to temperatures of about 30 to 60.degree. C., preferably to temperatures of 35 to 55.degree. C., and in a second stage immediately after leaving the reactor in the presence of water brought about 10 to 30 ° C, preferably to 15 to 25 ° C, lower temperatures.
  • the pressure can largely be chosen arbitrarily, but it is recommended to use it at normal pressure or only moderately reduced or increased pressure to work. Such pressures may occur by sucking or pushing the gases through the system.
  • the gas mixtures are preferably brought to the temperatures mentioned by washing them with aqueous washing liquids.
  • the gas mixtures emerging from the reactor contain water vapor in amounts sufficient to form an aqueous solution in which the 3-cyanopyridine, possibly present 3-methylpyridine, and the carbon dioxide and other by-products can be taken up, all that is required in the first stage cooling of the gas mixtures.
  • pure water can be used as the washing liquid in the first stage, it is generally expedient to use water which contains ammonia.
  • the amount and the amount of ammonia used in the washing liquid may depend on the composition of the gas mixtures to be treated, primarily on the content of water, ammonia and carbon dioxide. In most cases, especially in a continuous mode of operation in which the washing liquid is circulated, it is expedient to use water as washing liquid which is largely or completely saturated with ammonia at the temperature in question. It is advantageous to measure the washing liquid so that at least about 3 moles, preferably at least about, per mole of carbon dioxide in the gases to be treated. 5 moles of ammonia and about 0.1 to 0.5 liters of water per mole of ammonia are present.
  • the second stage is called washing liquid water is used which is free of ammonia ammonia or at most has a low ammonia content.
  • the washing liquid is expediently dimensioned such that at least about 0.2 liters of water are present per mole of ammonia in the gas mixture to be treated in the second stage.
  • the aqueous solution obtained in the first stage contains the 3-cyanopyridine, any unreacted 3-methylpyridine, ammonia, the carbon dioxide, this as ammonium bicarbonate, and the other by-products, insofar as they are soluble in the medium.
  • the aqueous solution obtained in the second stage contains ammonia.
  • the 3-cyanopyridine and optionally the 3-methylpyridine from the aqueous solution obtained in the first stage, it is extracted with an organic solvent.
  • suitable solvents are aliphatic chlorinated hydrocarbons or aromatic, optionally chlorinated, hydrocarbons, preferably benzene.
  • the extract is fractionally distilled.
  • the solvent recovered here can be used for further extractions.
  • the aqueous solution remaining after the extraction contains ammonium hydrogen carbonate in addition to ammonia.
  • the carbon dioxide is desorbed from this solution in that the solution, expediently with the addition of water, under pressures of approximately 5 to 12 bar, preferably 6 to 10 bar, at temperatures of approximately 120 to 170 ° C., preferably 130 to 160 ° C, is treated.
  • the carbon dioxide escapes with portions of water. It is generally advantageous to use coals to drive off dioxide and water to such an extent or water to such an extent.
  • Add amounts that a residual solution is obtained which contains about 2 to 10 moles, preferably 3 to 8 moles, of ammonia per liter of water and at most about 0.4 moles, preferably at most 0.3 moles, of carbon dioxide per mole of ammonia.
  • Such a residual solution is generally immediately suitable for use as a washing liquid in the first stage.
  • the aqueous solution obtained in the second stage is used to obtain the ammonia at temperatures of approximately 80 to 140 ° C., preferably 90 to 130 ° C., and pressures approximately 1.5 to 3.0 bar, preferably 1.8 to 2.7 bar, desorbed.
  • the ammonia obtained here can be recycled immediately and used for new reactions, and the water freed from the ammonia can be used as the washing liquid in the second stage.
  • the residual gas (31) from the gas scrubber (10) in the first stage is fed to the gas scrubber (30) in the second stage, which is operated at a temperature which is 10 to 30 ° C. lower than the gas scrubber (10) in the first stage.
  • the water (36) freed from ammonia in the desorption (35) is applied as a washing liquid to the gas scrubber (30).
  • the residual gas (34) remaining after washing in (30) is discarded.
  • the aqueous ammonia solution (32) flowing out of the gas scrubber (30) is fed to the desorption (35) in order to abort the ammonia.
  • the stripped ammonia (37) is returned to the reaction.
  • a device as shown in the figure was used.
  • the gas washers (10) and (30) consisted of packed columns.
  • An hourly gas mixture of 4800 normal liters of air, 13.5 kg of water, 12.7 kg of ammonia and 11.0 kg of 3-methylpyridine was reacted in an upstream reactor.
  • a portion of the gas mixture of 8.1 kg ammonia per hour and 12.6 kg water was exhaust gas (37) from the desorption. (35).
  • the reaction was carried out on a fixed bed catalyst which was prepared in accordance with DE-OS 3107755, Example 1.
  • the gas mixture (11) formed during the reaction essentially contained 84.4 kg of nitrogen, 14.4 kg of oxygen, 22.9 kg of water, 9.0 kg of ammonia, 1.1 kg of 3-methylpyridine and 9.9 kg of hourly -Cyanpyridine and 4.5 kg of carbon dioxide.
  • the gas mixture (11) was washed with 129.5 kg of solution (12) from (20) per hour at 50 ° C.
  • the solution contained 9.9 kg of ammonia and 4.6 kg of carbon dioxide per hour.
  • the gas scrubber (10) produced 165.7 kg of solution (13) per hour. It contained 12.3 kg of ammonia, 1.1 kg of 3-methylpyridine, 9.9 kg of 3-cyanopyridine and 8.9 kg of carbon dioxide per hour.
  • this solution was extracted with 93.1 kg of benzene (14) per hour.
  • the extract (16) contained 9.8 kg of 3-cyanopyridine per hour, corresponding to a yield of 99%, based on the 3-cyanopyridine supplied with the gas mixture (11), and also 1.5 kg of 3-methylpyridine.
  • the extract was fractionally distilled to obtain 3-cyanopyridine and 3-methylpyridine and to recover benzene.
  • the benzene was returned to the extraction and with 0.4 kc fresh benzene added every hour.
  • Carbon dioxide was stripped from the aqueous phase (17) of the extraction (15) in the desorption (20) at 8 bar and 145 ° C.
  • the exhaust gas (21) contained 3.3 kg of carbon dioxide per hour and also 0.3 kg of ammonia, 1.9 kg of water, 0.1 kg of 3-cyanopyridine and 0.4 kg of benzene. 7.9 kg of water (18) were added to the desorption (20) every hour.
  • the residual solution (12), which ran from the desorption (20) contained 12.0 kg of ammonia and 5.6 kg of carbon dioxide per hour on 139.5 kg of water. A portion of 82.5% of it was added as washing liquid to the first gas scrubber (10), the remaining portion of 17.5% was added to the desorption (35) (33).
  • the second gas washer (30) was operated at 35 ° C.
  • the residual gas (31) was introduced into this from the first gas scrubber (10), which contained 6.6 kg of ammonia per hour in addition to 0.2 kg of carbon dioxide. This gas was washed in (30) with 96.0 kg of ammonia-free water (36) in the desorption (35).
  • the exhaust gas (34) from the gas scrubber (30) contained 0.6 kg of ammonia per hour. It was fed to a combustion together with the exhaust gas (21) from (20).
  • the washing liquid (32) from the second gas scrubber (30) contained 6.0 kg of ammonia and 0.2 kg of carbon dioxide per hour. It was fed to desorption (35) and freed from ammonia at 2.2 bar and 108 ° C. The liquid (36) that was withdrawn from the desorption was virtually free of ammonia and carbon dioxide. An hourly portion of 4.9 kg was discarded by it as waste water (38), another portion (18) was added to the desorption (20) and the rest as washing liquid to the second gas scrubber (30) fed.
  • the gas (37) obtained from the desorption (35) contained 12.6 kg of water, 8.1 kg of ammonia and 1.2 kg of carbon dioxide per hour. It was returned to the reactor.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pyridine Compounds (AREA)
  • Treating Waste Gases (AREA)
  • Liquid Crystal Substances (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
EP82105359A 1981-07-22 1982-06-18 Procédé de préparation de 3-cyanopyridine Expired EP0070395B1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AT82105359T ATE22075T1 (de) 1981-07-22 1982-06-18 Verfahren zur gewinnung von 3-cyanpyridin.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19813128956 DE3128956A1 (de) 1981-07-22 1981-07-22 Verfahren zur gewinnung von 3-cyanpyridin
DE3128956 1981-07-22

Publications (3)

Publication Number Publication Date
EP0070395A2 true EP0070395A2 (fr) 1983-01-26
EP0070395A3 EP0070395A3 (en) 1983-07-20
EP0070395B1 EP0070395B1 (fr) 1986-09-10

Family

ID=6137480

Family Applications (1)

Application Number Title Priority Date Filing Date
EP82105359A Expired EP0070395B1 (fr) 1981-07-22 1982-06-18 Procédé de préparation de 3-cyanopyridine

Country Status (12)

Country Link
US (1) US4482719A (fr)
EP (1) EP0070395B1 (fr)
JP (1) JPS5824564A (fr)
AT (1) ATE22075T1 (fr)
AU (1) AU557923B2 (fr)
BR (1) BR8204175A (fr)
CA (1) CA1169864A (fr)
DE (2) DE3128956A1 (fr)
ES (1) ES512147A0 (fr)
IL (1) IL65844A (fr)
IN (1) IN155430B (fr)
ZA (1) ZA823553B (fr)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4603207A (en) * 1985-10-24 1986-07-29 The Standard Oil Company Conversion of a mixture of 3-methylpyridine and 3-methylpiperidine to 3-cyanopyridine
US4876348A (en) * 1985-10-29 1989-10-24 The Standard Oil Company Process for making 3-cyanopyridine
JPH0449209Y2 (fr) * 1987-02-09 1992-11-19
DE3866774D1 (de) * 1987-05-12 1992-01-23 Nippon Catalytic Chem Ind Verfahren zur herstellung aromatischer oder heterocyclischer nitrile.
DE19504283A1 (de) * 1995-02-09 1996-08-14 Degussa Verfahren zur Herstellung von Cyanopyridinen und dafür geeignete Katalysatoren
DE19647527C1 (de) * 1996-11-16 1998-03-12 Degussa Verfahren zur Herstellung von Cyanoverbindungen durch Ammonoxidation
JP4747417B2 (ja) * 2000-04-04 2011-08-17 三菱瓦斯化学株式会社 ニトリル化合物の製造方法
AT411384B (de) * 2000-04-10 2003-12-29 Hoerbiger Ventilwerke Gmbh Dichtring-kombination
DE10335454A1 (de) * 2003-08-02 2005-02-24 Reilly Industries, Inc., Indianapolis Verfahren zur Herstellung von Cyanopyridinen und dafür geeignete Katalysatoren
EP2319833A1 (fr) 2009-10-16 2011-05-11 Lonza Ltd. Procédés et dispositifs pour la production de solutions aqueuses de cyanopyridines
CN103467370B (zh) * 2013-09-12 2015-07-22 南通天泽化工有限公司 氰基吡啶及其衍生物的合成方法
CN104356061A (zh) * 2014-10-23 2015-02-18 河南省科学院高新技术研究中心 一种2-氰基吡啶高效吸收方法
CN112547042A (zh) * 2020-12-10 2021-03-26 中触媒新材料股份有限公司 一种2-氰基吡啶催化剂的制备方法

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE862011C (de) * 1949-06-21 1953-01-08 Nepera Chemical Co Inc Verfahren zur Herstellung von Pyridinabkoemmlingen
GB777746A (en) * 1954-12-09 1957-06-26 Distillers Co Yeast Ltd Process for the production of cyanopyridines
US2861999A (en) * 1956-03-27 1958-11-25 Allied Chem Production of cyanopyridines
DE2039497C3 (de) * 1970-08-08 1974-01-17 Deutsche Gold- Und Silber-Scheideanstalt Vormals Roessler, 6000 Frankfurt Verfahren zur Herstellung von Antimon enthaltenden Katalysatoren und Verwendung der Katalysatoren für die Herstellung von aromatischen und heteroaromatischen Nitrilen
CH582151A5 (fr) * 1973-08-10 1976-11-30 Lonza Ag
US3929811A (en) * 1973-11-15 1975-12-30 Lummus Co Production of pyridine nitriles and carboxylic acids

Also Published As

Publication number Publication date
DE3273159D1 (en) 1986-10-16
EP0070395A3 (en) 1983-07-20
ZA823553B (en) 1983-03-30
IL65844A (en) 1985-07-31
IN155430B (fr) 1985-01-26
ES8500237A1 (es) 1984-10-01
AU8608682A (en) 1983-01-27
CA1169864A (fr) 1984-06-26
JPS5824564A (ja) 1983-02-14
EP0070395B1 (fr) 1986-09-10
ATE22075T1 (de) 1986-09-15
IL65844A0 (en) 1982-08-31
DE3128956A1 (de) 1983-02-10
US4482719A (en) 1984-11-13
JPH0414108B2 (fr) 1992-03-11
AU557923B2 (en) 1987-01-15
ES512147A0 (es) 1984-10-01
BR8204175A (pt) 1983-07-12

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